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通过带有附加芳基的钌(II)菲咯啉配合物实现长寿命LC态的获取。

Accessing a Long-Lived LC State in a Ruthenium(II) Phenanthroline Complex with Appended Aromatic Groups.

作者信息

Shillito Georgina E, Bodman Samantha E, Mapley Joseph I, Fitchett Christopher M, Gordon Keith C

机构信息

Department of Chemistry, University of Otago, P.O. Box 56, Dunedin 9001, New Zealand.

School of Physical and Chemical Sciences, University of Canterbury, Private Bag 4800, Christchurch 8041, New Zealand.

出版信息

Inorg Chem. 2020 Dec 7;59(23):16967-16975. doi: 10.1021/acs.inorgchem.0c02102. Epub 2020 Nov 11.

Abstract

The photophysical properties of a series of heteroleptic Ru(II) complexes of the form [Ru(phen)(phen-5,6-R)], where phen = 1,10-phenanthroline and R = phenyl (Ph), --butylbenzene (-Ph-tBu), -methoxybenzene (-Ph-OMe), and 2-naphthalene (2-naph), have been measured. Variation of the R group does not greatly perturb the electronic properties of the ground state, which were explored with electronic absorption and resonance Raman spectroscopy and are akin to those of the archetypal parent complex [Ru(phen)]. All complexes were shown to possess emissive MLCT states, characterized through transient absorption and emission spectroscopy. However, an additional, long-lived excited state was observed in the Ru(II) naphthalene complex. The naphthalene substituents facilitate population of a 40 μs dark state which decays independently to that of the emissive MLCT state. This state was characterized as LC in nature, delocalized over the naphthalene substituted ligand.

摘要

已对一系列通式为[Ru(phen)(phen - 5,6 - R)]的杂配Ru(II)配合物的光物理性质进行了测定,其中phen = 1,10 - 菲咯啉,R = 苯基(Ph)、对叔丁基苯(-Ph - tBu)、对甲氧基苯(-Ph - OMe)和2 - 萘基(2 - nap)。R基团的变化对基态的电子性质影响不大,通过电子吸收光谱和共振拉曼光谱对其进行了探究,其与原型母体配合物[Ru(phen)]的电子性质相似。所有配合物均显示具有发光的金属 - 配体电荷转移(MLCT)态,通过瞬态吸收光谱和发射光谱对其进行了表征。然而,在Ru(II)萘配合物中观察到了另一种长寿命激发态。萘取代基有利于一个40 μs暗态的形成,该暗态独立于发光的MLCT态进行衰减。该态本质上被表征为配体中心(LC)态,在萘取代配体上离域。

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